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Caption : Accreditation =Accreditation
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    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of recurrent mutation of the MED12 gene
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Paxis und Labor Dr. med Karl Mehnert
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays
    • Universität Zürich
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Universität Zürich
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of X-linked mental retardation MRXS14 (UPF3B gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Lujan-Fryns Syndrome (MED12, UPF3B and ZDHHC9 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of X-linked Intellectual Deficit, Raymond type (ZDHHC9 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Intellectual Deficit with Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of X-linked Intellectual Deficit due to X-chromosome Inactivation (RFLP and methylation analysis of x-chromosome)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Groningen
    • GRONINGEN
    • Accreditation
    • Molecular diagnosis of Lujan syndrome (MED12 gene)
    • UMCG - Universitair Medisch Centrum Groningen
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of FG syndrome / Lujan-Fryns syndrome (MED12 gene (exon 21,22) and UPF3B gene)
    • Praxis für Humangenetik Freiburg
    • More information
    • ITALY
    • LOMBARDIA
    • CREMONA
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Azienda Ospedaliera Istituti Ospitalieri di Cremona
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of FG syndrome / Lujan-Fryns syndrome (MED12 gene: exon 21 and 22)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of X-linked mental retardation with marfanoid habitus (ZDHHC9 gene)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of X-linked mental retardation MRXS14 (UPF3B gene)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 and UPF3B gene: total sequencing)
    • CHRU de Tours - Hôpital Bretonneau
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Praxis für Humangenetik
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Intellectual deficit, X-linked, Raymond type (ZDHHC9 gene: Sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of Lujan-Fryns syndrome (MED12 gene)
    • Institut für Klinische Genetik Bonn
    • More information
    • FRANCE
    • BOURGOGNE
    • DIJON
    • Molecular diagnosis of marfanoid syndromes with intellectual disabilities (MED12, ZDHHC9, UPF3B genes sequencing: entire coding region)
    • CHU de Dijon - Plateau technique de Biologie
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of marfanoid habitus - intellectual deficit, X-linked (MED12 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of X-linked intellectual deficit - marfanoid habitus (MED12 gene): analysis of 7 exons
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of Opitz-Kaveggia and Lujan-Frins syndromes (MED12 gene)
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • More information